Dr.Jart Every Sun Day Sun Fluid

Product NDC
49404-144
11-digit product format
494040144
Labeler code
49404
Product ID
49404-144_f05dd0e0-0381-78d5-e053-2995a90a99e2
Type
HUMAN OTC DRUG
Nonproprietary name
Homosalate, Octinoxate, Octisalate, Octocrylene, Avobenzone
Dosage form
LIQUID
Route
TOPICAL
Labeler
Have & Be Co., Ltd.
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2019-10-31
Marketing end
0000-00-00
Substance
AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OCTOCRYLENE
Active strength
3 mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
49404-144-022024-01-30C16284748780-11030e365-6d62-111a-e063-dadaa90a10e2Dr.Jart Every Sun Day Sun Fluid

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49404-144DR.JART EVERY SUN DAY SUN FLUID (HOMOSALATE, OCTINOXATE, OCTISALATE, OCTOCRYLENE, AVOBENZONE) LIQUID [HAVE & BE CO., LTD.]3Legacy NDC20240621_030dd13e-f33c-47c1-945e-fa58e3595517.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
49404-144-02494040144021 CONTAINER in 1 CARTON (49404-144-02) > 100 mL in 1 CONTAINER (49404-144-01) 1 container2019-10-310000-00-00NoNoCurrent